This page is intended for researchers supporting preclinical and early clinical GLP-1 programs who are selecting or validating assays to evaluate hydration status and vasopressin signaling during method development and data generation.
You’re likely in the right place if…
- GLP-1 treatment appears to affect fluid balance or hydration status
- Direct vasopressin (AVP) measurement is unstable or difficult to reproduce
- Longitudinal studies require a biomarker with high analytical stability
- Vasopressin signaling needs to be evaluated alongside metabolic outcomes
- Your program is advancing through preclinical or early clinical stages
Available Copeptin ELISA Kits
The following ELISA kits are commonly used for quantitative copeptin measurement in metabolic, endocrine, and translational research workflows.
Tip: Human sandwich ELISA kits are commonly used as a starting point for GLP-1 metabolic and hydration studies.
About these products
LS Bio is part of the Vector Laboratories family of companies. These copeptin ELISA kits are developed and sold by LS Bio and are linked here to support GLP-1-related metabolic and hydration research.
Species | Assay Type | Detection Range | Sample Types | Format | LS Bio Product (ELISA Kit) |
|---|---|---|---|---|---|
Human | Sandwich ELISA | 7.8 – 500 pg/mL | Plasma, Serum, Tissue Homogenates | 96-well plate | |
Human | Sandwich ELISA | 250 – 5,000 pg/mL | Plasma, Serum, Cell Culture Supernatants | 96-well plate | |
Human | Sandwich ELISA | 31.25 – 2,000 pg/mL | Plasma, Serum, Tissue Homogenates | 96-well plate |
All kits are for research use only.
Need a quick reference?
Download the Copeptin ELISA flyer for a concise overview of assay formats, detection ranges, and sample compatibility commonly used in preclinical and early clinical research.
Download Copeptin ELISA Flyer (PDF)Why Copeptin Instead of Direct Vasopressin (AVP)
Copeptin is derived from the same precursor as vasopressin but offers significantly greater stability in blood samples. Unlike AVP, copeptin concentrations are less sensitive to pre-analytical handling, enabling reproducible measurement across multiple timepoints during early-stage research.
